- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00313040
Study to Promote Physical Activity Among Overweight Persons
Promoting Increased Physical Activity as the Main Outcome of Treatment for Overweight Persons: A Pilot Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
OBJECTIVE: Epidemiologic evidence suggests that overweight persons who engage in modest amounts of physical activity - even that insufficient to produce or maintain weight loss - are at significantly reduced risk for health complications including all-cause mortality. Interventions for overweight persons targeting increased physical activity rather than weight loss as the main outcome of treatment have not been well studied and could represent simpler, more sustainable, and more cost-effective approaches in addressing the obesity epidemic.
METHOD: Pilot randomized controlled trial. Sedentary patients with BMI 25-45, and no major contraindications for unsupervised physical activity recruited. Participants randomized to receive either brief consultation consisting of 3 in-person meetings, a workbook, and limited telephone contact or usual care with their medical provider including access to community weight-loss groups/resources. Intervention therapists novice pre-professional students. The intervention is manualized and coded for treatment integrity. The main outcome measures are Cohen's d effect sizes and 95% confidence intervals for the change in moderate-equivalent intensity physical activity/week at 3 months relative to baseline assessed by a blinded assessor using the Stanford 7-Day Physical Activity Recall. Secondary outcomes include effect sizes and confidence intervals for changes in cardiorespiratory fitness and depression using the modified Canadian Aerobic Fitness test and Beck Depression Inventory. Analyses to be performed by intention to treat. Missing data to be imputed by baseline observation carried forward.
Study Type
Enrollment
Phase
- Phase 2
- Phase 1
Contacts and Locations
Study Locations
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California
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Stanford, California, United States, 94305-5722
- Stanford University Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- BMI 25-45
- not regularly physically active by staging algorithm (Norman et al,1998)
- AHA/ACSM risk class A1-A3 apparently healthy with no contraindications to medically unsupervised physical activity
- physician consent
Exclusion Criteria:
- BMI<25; BMI>45
- regularly physically active by staging algorithm (Norman et al,1998)
- AHA/ACSM risk class B or C contraindication for medically unsupervised physical activity
- physician will not consent
- diagnosis of dementia, psychotic disorder
- legal guardian or conservator appointed
- anorexia
- bulimia
- live more than one hour commute from Stanford
- no reliable means of transportation to scheduled appointments at Stanford
- unable to followup for duration of study period as result of planned move
- female and sexually active without birth control or planning to become pregnant
- unable to read and write in English
- friend or family member of enrolled participant
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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Effect size and 95% CI for change in Physical Activity by 7 Day Physical Activity Recall at 3 months between groups
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Secondary Outcome Measures
Outcome Measure |
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Effect size and 95% CI for change in Cardiorespiratory Fitness at 3 months by modified Canadian Aerobic Fitness Test
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Effect size and 95% CI for change in Depression by Beck Depression Inventory at 3 months
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Physical Activity Staging Algorithm (Norman, 1998)
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Motives for Physical Activity Measure (Ryan et al, 1997)
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Self Efficacy for Overcoming Barriers to Exercise (Garcia and King, 1991)
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Outcomes Expectancies for Exercise (Mascola 2004)
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Health Care Climate Questionnaire (Williams, 1996)
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General Causality Orientations Scale (Deci and Ryan)
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Treatment Self Regulation Questionnaire (Deci and Ryan)
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Mediators of Exercise Questionnaire (Mascola)
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Cholestech LDX lipoprotein and glucose profile
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Resting Heart Rate
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Blood Pressure Omron automated sphygmomanometer
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Waist Circumference
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Percent Body Fat Omron bioelectric impedence
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Polar OwnIndex score
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Anthony J Mascola, MD, Stanford University
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 79940
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